114937-04-1

Basic information

• Product Name: (4R)-2-<(1S)-1-(4-(2-Methylpropyl)phenyl)ethyl>thiazolidine-4-carboxylic Acid
• CAS NO: 114937-04-1
• Molecular Weight: 293.43
• Mol File: 114937-04-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (4R)-2-<(1S)-1-(4-(2-Methylpropyl)phenyl)ethyl>thiazolidine-4-carboxylic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4R)-2-<(1S)-1-(4-(2-Methylpropyl)phenyl)ethyl>thiazolidine-4-carboxylic Acid(114937-04-1)
• EPA Substance Registry System: (4R)-2-<(1S)-1-(4-(2-Methylpropyl)phenyl)ethyl>thiazolidine-4-carboxylic Acid(114937-04-1)

Safety Data

• Hazardous Substances Data: 114937-04-1(Hazardous Substances Data)

Upstream product

• 114937-30-3 (2S)-2-<4-(2-Methylpropyl)phenyl>propan-1-ol 
• 81576-55-8 (S)-(+)-methyl 2-(4-isobutylphenyl)propionate 
• 51146-56-6 (S)-ibuprofen 
• 52-89-1 l-cysteine hydrochloride 
• 110773-62-1 S-2-(p-isobutylphenyl)propionaldehyde 
• 93673-13-3 (2R)-2-<4-(2-methylpropyl)phenyl>propan-1-ol 
• 81576-57-0 (R)-ibuprofen methyl ester 
• 51146-57-7 (R)-ibuprofene 
• 114937-27-8 (2R)-2-<4-(2-Methylpropyl)phenyl>propanal 
• 61566-34-5 (+/-)-ibuprofen methyl ester 
• 15687-27-1 ibuprofen 
• 36039-36-8 2-(4-isobutylphenyl)propan-1-ol 

Relevant articles and documents

Synthesis and in solution behaviour of new 2-substituted-4-thiazolidinecarboxylic acid derivatives

A number of 2-substituted-4-thiazolidinecarboxylic acid derivatives were synthesized by cyclocondensation of L-cysteine or its esters with various aldehydes, resulting from acids provided with antiinflammatory properties. In the cyclocondensation a new chiral center at C-2 position of thiazolidine ring is formed giving rise to a mixture of diastereoisomers which can be partially separated. These diastereoisomers show in solution a fast epimerisation at the same chiral center as evidenced by 1H-nmr studies.